Product Recalls in North Dakota
Product recalls affecting North Dakota — including food, drugs, consumer products, medical devices, and vehicles distributed to North Dakota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,404 recalls have been distributed to North Dakota in the last 12 months.
Showing 20481–20500 of 27,512 recalls
Recalled Item: Anesthesia device service kits. ASSY-MSN Recalled by GE Medical Systems, LLC...
The Issue: The Drive Gas Check Valve of certain Anesthesia products could become stuck...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FMC7 FITC Recalled by Becton, Dickinson and Company, BD Biosciences Due to...
The Issue: Becton, Dickinson and Company (BD) has determined that the FMC7 FITC (ASR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CDI¿ H/S Cuvette The intended use for the CDI¿ H Recalled by Terumo...
The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received complaints of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IBA Dosimetry GmbH Lift Table Type 4320 Recalled by Iba Dosimetry Gmbh Due...
The Issue: When the electric lift table is connected to the mains power, in a very rare...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flow-i Anesthesia System Product Usage: The indication for the Flow-i...
The Issue: Electrical issues in the control, monitoring or panel sub-systems, caused by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOSAIQ Oncology Information System MOSAIQ is an oncology information system...
The Issue: Incorrect drug dosage due to "Age Limit" and patient weight data item issue.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Lumify Diagnostic Ultrasound Recalled by Philips Ultrasound, Inc....
The Issue: Color Flow direction is displayed incorrectly in Lumify 1.0. The system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perkin Elmer WIZARD2 2-detector Recalled by Perkinelmer Due to The content...
The Issue: The content of the second #023 barcode ID label in the Barcode ID Label...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perkin Elmer WIZARD2 10-detector Recalled by Perkinelmer Due to The content...
The Issue: The content of the second #023 barcode ID label in the Barcode ID Label...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SYNTHECEL Dura Repair Recalled by Synthes (USA) Products LLC Due to It was...
The Issue: It was reported that the SYNTHECEL Dura Repair could adhere to various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perkin Elmer WIZARD2 1-detector Recalled by Perkinelmer Due to The content...
The Issue: The content of the second #023 barcode ID label in the Barcode ID Label...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SYNTHECEL Dura Repair Recalled by Synthes (USA) Products LLC Due to It was...
The Issue: It was reported that the SYNTHECEL Dura Repair could adhere to various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SYNTHECEL Dura Repair Recalled by Synthes (USA) Products LLC Due to It was...
The Issue: It was reported that the SYNTHECEL Dura Repair could adhere to various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perkin Elmer WIZARD2 10-detector Recalled by Perkinelmer Due to The content...
The Issue: The content of the second #023 barcode ID label in the Barcode ID Label...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perkin Elmer WIZARD2 5-detector Recalled by Perkinelmer Due to The content...
The Issue: The content of the second #023 barcode ID label in the Barcode ID Label...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SYNTHECEL Dura Repair Recalled by Synthes (USA) Products LLC Due to It was...
The Issue: It was reported that the SYNTHECEL Dura Repair could adhere to various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SYNTHECEL Dura Repair Recalled by Synthes (USA) Products LLC Due to It was...
The Issue: It was reported that the SYNTHECEL Dura Repair could adhere to various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perkin Elmer WIZARD2 1-detector Recalled by Perkinelmer Due to The content...
The Issue: The content of the second #023 barcode ID label in the Barcode ID Label...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perkin Elmer ClWIZARD2 5-detector Recalled by Perkinelmer Due to The content...
The Issue: The content of the second #023 barcode ID label in the Barcode ID Label...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAGNETOM systems Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Possible installation error of the quench lines of superconducting magnets,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.